Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.03 (T)
Location

Chromosome 20:9048472 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.9048472G>T

Variation displays